151135-82-9

• 

• Basic information

  1. Product Name: Kanzonol C
  2. Synonyms: Kanzonol C
  3. CAS NO:151135-82-9
  4. Molecular Formula: C25H28O4
  5. Molecular Weight: 392.49
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 151135-82-9.mol
  9. Article Data: 4

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 588.2±50.0 °C(Predicted)
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: 1.165±0.06 g/cm3(Predicted)
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. PKA: 7.95±0.40(Predicted)
  10. CAS DataBase Reference: Kanzonol C(CAS DataBase Reference)
  11. NIST Chemistry Reference: Kanzonol C(151135-82-9)
  12. EPA Substance Registry System: Kanzonol C(151135-82-9)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 151135-82-9(Hazardous Substances Data)

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• Article

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151135-82-9 Usage

General Description

Kanzonol C is a chemical compound that belongs to the class of quinones, which are known for their diverse biological activities. It is derived from natural sources such as plants and exhibits antioxidant, anti-inflammatory, and anti-cancer properties. Kanzonol C has been studied for its potential to inhibit the growth of cancer cells and reduce inflammation in various disease conditions. Its antioxidant properties also make it a potential candidate for therapeutic applications in oxidative stress-related disorders. Overall, Kanzonol C shows promise as a bioactive compound with potential pharmacological uses.

Check Digit Verification of cas no

The CAS Registry Mumber 151135-82-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,1,3 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 151135-82:
(8*1)+(7*5)+(6*1)+(5*1)+(4*3)+(3*5)+(2*8)+(1*2)=99
99 % 10 = 9
So 151135-82-9 is a valid CAS Registry Number.

151135-82-9Upstream product

• 1314539-20-2 2'-prenyloxy-4'-methoxymethoxyacetophenone 
• 65490-08-6 2-hydroxy-4-(methoxymethoxy)acetophenone 
• 54730-26-6 4-methoxymethoxy-3-(3,3-dimethylallyl)-2-hydroxyacetophenone 
• 74021-58-2 4-methoxymethoxy-3-(3-methyl-but-2-enyl)-benzaldehyde 
• 89024-12-4 (E)-1-(2-hydroxy-4-(methoxymethoxy)-3-(3-methylbut-2-en-1-yl)phenyl)-3-(4-(methoxymethoxy)-3-(3-methylbut-2-en-1-yl)phenyl)prop-2-en-1-one 
• 870-63-3 prenyl bromide 
• 115-18-4 2-methyl-3-buten-2-ol 
• 54730-30-2 4-hydroxy-3-C-prenylbenzaldehyde 
• 123-08-0 4-hydroxy-benzaldehyde 
• 19825-40-2 2,4-Dihydroxy-3-C-prenylacetophenone 
• 89-84-9 2',4'-dihydroxy-4-acetophenone 

151135-82-9Downstream Products

151135-82-9Relevant articles and documents

Synthetic method and application of natural product Kanzonol C and derivatives thereof

-

, (2019/12/02)

The invention discloses a synthetic method and application of a natural product Kanzonol C and derivatives thereof. The structural formula (I) and (II) are shown in the specification: compared with anatural product Kanzonol C, the obtained novel isopenten

Synthetic methods for prenylated chalcones and pyranochalcones

-

, (2017/04/27)

The inventors of the present invention invented a simple and effective way to synthesize compounds 1-9 of natural prenylated chalcones and pyrano chalcones by using Claisen-Schmidt condensation as a main step. In addition, an anti-inflammatory effect of synthetic compounds was evaluated in RAW 264.7 macrophages which were stimulated with a lipopolysaccharide. As a result, chalcone compounds having prenyl groups in a ring A (an acetophenone part) show weak inhibition or no inhibition on the generation of nitrogen oxide while chalcones (5, 6, 8, and 9) having no prenyl groups in the ring A show normal or good activity, and have no cytotoxicity.COPYRIGHT KIPO 2017

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